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filingDate 2001-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_343d6b76b19c90b98f824aaa3a354a92
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d94572349ca669e68c40ec5ee1aedcfd
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publicationDate 2003-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2003176449-A1
titleOfInvention 3-Phenyl-imidazo-pyrimidine derivatives as ligands for gaba receptors
abstract A class of 3-phenylimidazo(1,2-α) pyrimidine derivatives (of Formula I, or salt or prodrug thereof: I) wherein Y represents a chemical bond, an oxygen atom, or a —NH— linkage; Z represents an optionally substituted aryl or heteroaryl group; R 1 represents hydrogen, hydrocarbon, a heterocyclic group, halogen, cyano trifluoromethyl, nitro, —OR a , —SR a , —SOR a , —SO 2 R a , —SO 2 NR a R b , —NR a R b , —NR a COR b , —NR a CO 2 R b , —COR a , CO 2 R a , —CONR a R b or —CR a ═NOR b ; and R a and R b independently represent hydrogen, hydrocarbon or a heterocyclic group.), substituted at the meta position of the phenyl ring by an optionally substituted aryl or heteroaryl group which is directly attached or bridged by an oxygen atom or a —NH— linkage, are selective ligands for GABA A receptors, in particular having good affinity for the a2 and/or a3 and/or a5 subunit thereof, and are accordingly of benefit in the treatment and/or prevention of adverse conditions of the central nervous system, including anxiety, convulsions and cognitive disorders.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019099578-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007213338-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11673891-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005041971-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11730810-B2
priorityDate 2000-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 861.